المؤلفون: Ana Šmaguc, Danijela Petković Ramadža, Vladimir Sarnavka, Vjekoslav Krželj, Bernarda Lozić, Silvija Pušeljić, Valentina Rahelić, Nikola Mesarić, Marina Grubić, Ana Bogdanić, Anita Špehar Uroić, Tamara Žigman, Ruža Grizelj, Jurica Vuković, Duško Mardešić, Ildiko Szatmari, Isabel Rivera, Ksenija Fumić, Ivo Barić

المصدر: Liječnički vjesnik, Vol 145, Iss 1-2, Pp 1-11 (2023)

مصطلحات موضوعية: galactosemias – complications, diagnosis, genetics, galactose – blood, utp-hexose-1-phosphate uridylyltransferase – deficiency, udp glucose 4-epimerase – deficiency, galactokinase – deficiency, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://lijecnicki-vjesnik.hlz.hr/pdf/1-2-2023/01_smaguc.pdf; https://doaj.org/toc/0024-3477; https://doaj.org/toc/1849-2177

URL الوصول: https://doaj.org/article/172aeb75c94342c59411f163b00e629a

المؤلفون: Šmaguc, Ana, Ramadža, Danijela Petković, Sarnavka, Vladimir, Krželj, Vjekoslav, Lozić, Bernarda, Pušeljić, Silvija, Rahelić, Valentina, Mesarić, Nikola, Grubić, Marina, Bogdanić, Ana, Uroić, Anita Špehar, Žigman, Tamara, Grizelj, Ruža, Vuković, Jurica, Mardešić, Duško, Szatmari, Ildiko, Rivera, Isabel, Fumić, Ksenija, Barić, Ivo

المصدر: Liječnički vjesnik
Volume 145
Issue 1-2

مصطلحات موضوعية: GALACTOSEMIAS – complications, diagnosis, genetics, GALACTOSE – blood, UTP-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE – deficiency, genetics, UDP GLUCOSE 4-EPIMERASE – deficiency, genetics, GALACTOKINASE – deficiency, genetics, MUTATION, PHENOTYPE, NEONATAL SCREENING, CROATIA, Deskriptori GALAKTOZEMIJA – dijagnoza, genetika, komplikacije, GALAKTOZA – u krvi, GALAKTOZA-1-FOSFAT URIDIL TRANSFERAZA – genetika, nedostatak, URIDIN DIFOSFAT GALAKTOZA 4-EPIMERAZA – genetika, nedostatak, GALAKTOKINAZA – genetika, nedostatak, MUTACIJA, FENOTIP, NOVOROĐENAČKI PROBIR, HRVATSKA, GALAKTOZEMIJA – dijagnoza, genetika, komplikacije

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2810e5ec76630a5348344fd768c11311
https://www.bib.irb.hr/1263470

المؤلفون: Nathalie Vionnet, Kathryn J Burton, René Badertscher, Guy Vergères, Grégory Pimentel, Linda H. Münger, Carola Freiburghaus, François P. Pralong

المصدر: The American Journal of Clinical Nutrition
The American journal of clinical nutrition, vol. 109, no. 2, pp. 470-477

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, Genotype, medicine.medical_treatment, Medicine (miscellaneous), Lactose, lactase activity, Polymorphism, Single Nucleotide, Lactase activity, 03 medical and health sciences, chemistry.chemical_compound, Young Adult, 0302 clinical medicine, Blood serum, Lactose Intolerance, Internal medicine, medicine, Animals, Humans, milk digestion, Lactase, Lactose intolerance, Nutrition and Dietetics, Biomarkers/metabolism, Dairy Products/adverse effects, Digestion/genetics, Galactitol/blood, Galactitol/metabolism, Galactitol/urine, Galactose/blood, Galactose/metabolism, Galactose/urine, Lactase/deficiency, Lactase/genetics, Lactase/metabolism, Lactose/blood, Lactose/metabolism, Lactose/urine, Lactose Intolerance/genetics, Lactose Intolerance/metabolism, Liver, Milk/adverse effects, Milk/chemistry, Nutrition Assessment, Postprandial Period, Sugar Acids/blood, Sugar Acids/metabolism, Sugar Acids/urine, nutrigenetics, personalized nutrition, Galactitol, Galactose, Sugar Acids, medicine.disease, Lactase persistence, Original Research Communications, 030104 developmental biology, Postprandial, Endocrinology, Milk, chemistry, 030211 gastroenterology & hepatology, Digestion, Dairy Products, galactose metabolism, Biomarkers

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34df8560632f3eb76ce087d516d799a9
http://europepmc.org/articles/PMC6367971

المؤلفون: Kathryn J Burton, Ueli von Ah, René Badertscher, Nathalie Vionnet, Grégory Pimentel, Gilbert Greub, Carola Freiburghaus, François P. Pralong, Marta Rosikiewicz, Linda H. Münger, Guy Vergères

المصدر: The British journal of nutrition, vol. 118, no. 12, pp. 1070-1077

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, Adolescent, Veillonella, Medicine (miscellaneous), Lactose, Urine, 03 medical and health sciences, chemistry.chemical_compound, Feces, Young Adult, Double-Blind Method, Internal medicine, medicine, Ingestion, Animals, Humans, Intestinal Mucosa, Alleles, Nutrition and Dietetics, Intestinal permeability, Cross-Over Studies, biology, Galactose, medicine.disease, biology.organism_classification, Postprandial Period, Yogurt, beta-Galactosidase, Diet, Gastrointestinal Microbiome, Intestines, Lactase persistence, 030104 developmental biology, Endocrinology, Postprandial, Milk, chemistry, Feces/microbiology, Galactose/blood, Intestines/metabolism, Intestines/microbiology, Lactose/blood, Veillonella/isolation & purification, beta-Galactosidase/genetics, beta-Galactosidase/metabolism, FDR false discovery rate, Lactosaemia

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5db154c878fe5e28b6e7cf75e626fdd6
https://serval.unil.ch/notice/serval:BIB_45226C6B180A

المؤلفون: Olaniyi, S.K., Usman, T.O., Adeyanju, O.A., Salman, T.M., Olatunji, L.A.

المصدر: Tropical Journal of Health Sciences; Vol 24, No 3 (2017); 27-32

مصطلحات موضوعية: Glucose, fructose, galactose, blood glucose, gastric secretion, ulcer score

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=78975075580c::e44b97615f658adae7e969771491878a
https://www.ajol.info/index.php/tjhc/article/view/159487

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عناروين إضافية: Experiences with galactosemia in Croatia

المصدر: Liječnički vjesnik; ISSN 0024-3477 (Print); ISSN 1849-2177 (Online); Volume 145; Issue 1-2

مصطلحات الفهرس: Deskriptori GALAKTOZEMIJA – dijagnoza, genetika, komplikacije; GALAKTOZA – u krvi; GALAKTOZA-1-FOSFAT URIDIL TRANSFERAZA – genetika, nedostatak; URIDIN DIFOSFAT GALAKTOZA 4-EPIMERAZA – genetika, nedostatak; GALAKTOKINAZA – genetika, nedostatak; MUTACIJA; FENOTIP; NOVOROĐENAČKI PROBIR; HRVATSKA, GALACTOSEMIAS – complications, diagnosis, genetics; GALACTOSE – blood; UTP-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE – deficiency, genetics; UDP GLUCOSE 4-EPIMERASE – deficiency, genetics; GALACTOKINASE – deficiency, genetics; MUTATION; PHENOTYPE; NEONATAL SCREENING; CROATIA, text, info:eu-repo/semantics/article, info:eu-repo/semantics/publishedVersion

URL: https://hrcak.srce.hr/294579
https://hrcak.srce.hr/file/433204
info:eu-repo/semantics/altIdentifier/doi/10.26800/LV-145-1-2-1

المؤلفون: FREZAL J, REY J

المصدر: La Medecine infantile [Med Infant (Paris)] 1962 May; Vol. 69, pp. 303-13.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Librairie Maloine Country of Publication: France NLM ID: 2985233R Publication Model: Print Cited Medium: Print ISSN: 0025-6773 (Print) Linking ISSN: 00256773 NLM ISO Abbreviation: Med Infant (Paris) Subsets: OLDMEDLINE

مواضيع طبية MeSH: Carbohydrate Metabolism* , Galactosemias*, Fructose/*metabolism , Galactose/*blood, Humans